Mansouri Ladan, Lundwall Kristina, Moshfegh Ali, Jacobson Stefan H, Lundahl Joachim, Spaak Jonas
Immunology and Allergy Unit, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Sciences, Karolinska Institutet, Danderyd University Hospital, Stockholm, Sweden.
BMC Nephrol. 2017 May 16;18(1):161. doi: 10.1186/s12882-017-0576-8.
Chronic kidney disease (CKD) is a major risk factor for cardiovascular disease (CVD), partly due to endothelial dysfunction and chronic inflammation. Vitamin D treatment in end stage renal disease is suggested to modulate the immune system and lead to improved outcomes. We and others have demonstrated that treatment with vitamin D or activated vitamin D analogues protects the endothelial function in less severe renal disease as well. Since the endothelial protection might be mediated by vitamin D effects on inflammation, we assessed levels of pro-inflammatory cytokines and micro RNAs (miRs) in patients with moderate CKD, treated with an active vitamin D analogue (paricalcitol).
Thirty-six patients with moderate CKD were randomized to 12 weeks treatment with placebo, 1 μg, or 2 μg paricalcitol daily. Cytokines were measured by Milliplex 26-plex. Total RNA was isolated from plasma and miRs were determined by quantitative reverse transcription PCR analysis.
Selected pro-inflammatory cytokines decreased significantly following treatment, while no change was observed in the placebo group. The micro RNAs; miR 432-5p, miR 495-3p, and miR 576-5p were significantly downregulated in the active treated groups, compared to the placebo group.
Paricalcitol treatment for 12 weeks in patients with moderate CKD reduces cytokines and micro RNAs involved in atherosclerosis and inflammation. The potentially protective role of vitamin D receptor activation in the inflammatory processes regarding the long-term outcomes in CKD patients warrants further studies.
SOLID study; NCT01204528 , April 27, 2010.
慢性肾脏病(CKD)是心血管疾病(CVD)的主要危险因素,部分原因是内皮功能障碍和慢性炎症。建议在终末期肾病中使用维生素D治疗来调节免疫系统并改善预后。我们和其他人已经证明,维生素D或活性维生素D类似物治疗在较轻的肾脏疾病中也能保护内皮功能。由于内皮保护可能是由维生素D对炎症的作用介导的,我们评估了接受活性维生素D类似物(帕立骨化醇)治疗的中度CKD患者中促炎细胞因子和微小RNA(miRs)的水平。
36例中度CKD患者被随机分为三组,分别接受为期12周的安慰剂、每日1μg或2μg帕立骨化醇治疗。通过Milliplex 26-通道检测法测定细胞因子。从血浆中分离总RNA,并通过定量逆转录PCR分析测定miRs。
治疗后选定的促炎细胞因子显著降低,而安慰剂组未观察到变化。与安慰剂组相比,活性治疗组中的微小RNA;miR 432-5p、miR 495-3p和miR 576-5p显著下调。
中度CKD患者接受12周的帕立骨化醇治疗可降低参与动脉粥样硬化和炎症的细胞因子和微小RNA。维生素D受体激活在CKD患者长期预后的炎症过程中的潜在保护作用值得进一步研究。
SOLID研究;NCT01204528,2010年4月27日。